iridium(1V). An Organometallic Aryl Oxide ... - ACS Publications

A generous support from Mitsubishi Kasei Corporation is gratefully acknowledged. The authors (R.J.D. and W.R.S.) thank Dr. Zhaoda Zhang for his helpfu...
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J . Am. Chem. SOC.1992, 114, 6582-6583

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these novel SiCAC reactions have high synthetic potential, further investigations on the mechanism, organometallic chemistry, and applications to organic syntheses are actively underway. Acknowledgment. This research was supported by grants from the National Science Foundation and the National Institutes of Health. A generous support from Mitsubishi Kasei Corporation is gratefully acknowledged. The authors (R.J.D. and W.R.S.) thank Dr. Zhaoda Zhang for his helpful discussions as well as technical assistance. Supplementary Material Available: Identification data for 7, 9, 10, 11, and 13, including 2D N M R spectra, i.e., COSY and HETCOR, for 10 and 11 (7 pages). Ordering information is given

on any current masthead page. (8) The intramolecular trapping of a P-silylethenyl-nickel species by an alkyne moiety in 1,7-octadiyne and related systems, giving the corresponding carbocyclization product, was reported by Tamao et al. See: Tamao, K.; Kobayashi, K.; Ito, Y.J . Am. Chem. SOC.1989, 111, 6478.

Figure 1. View showing the structure of Ir(l,S-COD)(3,6-DBCat),. A crystallographic 2-fold axis passes between the olefin groups and relates the two catecholate ligands. Selected bond lengths (A):Ir-01 2.014 (7), Ir-02 2.014 (6),Ir-CIS 2.207 (ll), Ir-CI8 2.192 (9), C1-01 1.352 (13), C2-02 1.318 (12), C15-Cl8’ 1.413 (17).

for the complex in the solid state is consistent with the structural features of the quinone ligands. Ring C-C lengths reflect the expected aromatic structure of a catecholate ligand, and the C-O lengths are of values that are longer than semiquinone lengthss ( 1,5-Cyclooctadiene)bis( 3,6-di-tert-butylcatecholato)In particular, the length to 0 1 is 1.35 (1) A, while the length to iridium(1V). An Organometallic Aryl Oxide Complex 0 2 , trans to the COD olefin bond, is 1.32 (1) A. In toluene with a Charge-Transfer Transition at Unusually Low solution at room temperature, the S = complex molecule shows Energy a broad EPR resonance centered about a g-value of 1.986 which is approximately 200 G in width. In frozen toluene at 77 K, the Christopher W. Lange and Cortlandt G. Pierpont* signal splits to give a slightly rhombic spectrum with components gl = 1.948, gz = 1.952, and g3 = 2.006. No hyperfine structure Department of Chemistry and Biochemistry is observed for either the isotropic or anisotropic spectrum. University of Colorado, Boulder, Colorado 80309 Electrochemical characterization on Ir( 1,5-COD)(3,6-DBCat), Received February 19, 1992 shows that the complex undergoes reversible one-electron oxidation and reduction reactions.6 Couples are closely spaced at potentials Many of the interesting and important features of transition of -0.092 V and -0.636 V (vs Fc+/Fc), respectively, and the metal complexes containing catecholate and semiquinone ligands complex may be chemically oxidized with Ag(PF6) and reduced are related to the similarity in energy between quinone n*-orbitals with cobaltocene. and the metal d-levels. In some cases this property is responsible Figure 2 shows the infrared spectrum obtained for the complex.’ for intense, low-energy charge-transfer transitions that sometimes The sharp bands at lower energy are the usual ligand vibrations, extend well into the near-infrared NIR region.’ Characterization but the broad, intense transition centered near 4200 cm-l is an on the “bending crystals” of Rh(C0)2(3,6-di-tert-butylsemi- electronic absorption. The band appears unsymmetrical in the quinone) has shown that a low-energy metal-ligand chargefigure due to moisture in the KBr matrix; in toluene solution at transfer transition associated with stacked oligomers of complex room temperature it appears as a single symmetrical transition units contributes to unique photomechanical properties in the solid at 2340 nm with a molar extinction coefficient of 5100 M-’ cm-l. state.2 The higher d-orbital energy of iridium may result in Assignment of this transition is not unambiguous. It may simply charge-transfer transitions shifted further to lower energy, resulting be a metal-catecholate charge-transfer transition,* but other in compounds with high optical sensitivity in the infrared. We possibilities exist. Intense, low-energy interligand charge-transfer now describe an unusual product obtained by the addition of transitions commonly occur for members of the ML2(3,5cobaltocenium 3,6-di-tert-butylsemiquinoneto [Ir( 1,5-COD)C1I2. DBCat)(3,5-DBCat) series, with M = Ru and Os and Lz = bpy, The anticipated product of the synthetic procedure was Ir2PPh3, and 2C0.9J0 This requires significant mixing with an ( 1,5-COD)(3,6-DBSQ).3 However, crystallographic characIr(II1) charge-localized form of the complex, Ir( 1,5-COD)(3,6terization on the dark red complex obtained from this reaction DBSQ)(3,6-DBCat). The electrochemistry supports this in apshowed that the product was actually Ir(l,5-COD)(3,6-DBCat)2 with the structure shown in Figure 1.4 The Ir(1V) formulation (1) Haga, M.; Dodsworth, E. S.;Lever, A. B. P.; Bwne, S.R.; Pierpont, C. G . J . Am. Chem. SOC.1986, 108, 7413. (2) Lange, C. W.;Foldeaki, M.; Nevodchikov, V. I.; Cherkasov, V . K.; Abakumov, G. A.; Pierpont, C. G. J . Am. Chem. SOC.1992, 114, 4220. (3) Synthesis of Ir(l,S-COD)(3,6-DBCat),: [Ir(1,5-COD)CI], (0.153g, 0.23 mmol) dissolved in 5 mL of CH,CI, was added to a solution of [Co(Cp),](3,6-DBSQ) prepared by combining cobaltocene (0.091g, 0.48mmol) and 3,6-di-lerf-butyl-l,2-benzoquinone (0.10 g, 0.47 mmol) in 10 mL of CH2C12. The mixture became dark red, and a brown precipitate separated from the solution. The precipitate was collected by filtration, and the red filtrate was slowly evaporated under a flow of N2. Dark red crystals of Ir(l,5-COD)(3,6-DBCat), were obtained from the evaporated filtrate in yields that have varied from 30% to 50%. The brown precipitate has not yet been identified. Details of the reaction and products will be published separately. (4)X-ray analysis of Ir(l,5-COD)(3,6-DBCat),: tetragonal, space group P4,2,2;u = 15.007(2)A, c = 15.234 (4)A, V = 3431 (1) A’, 2 = 4;R = 0.040for 2261 unique observed reflections. Details of the structure determination are given in the supplementary material.

0002-786319211514-6582$03.00/0

(5) (a) Pierpont, C. G.; Buchanan, R. M. Coord. Chem. Reo. 1981, 38, 44. (b) Carugo, 0.;Castellani, C. B.; Djinovic, K.; Rizzi, M. J . Chem. SOC., Dalfon Trans. 1992, 837. (6)Cyclic voltammograms were recorded in acetonitrile solution using tetrabutylammonium hexafluorophosphate as electrolyte. An Ag/Ag+ reference electrode was used, and the cobaltocenium/cobaltocenecouple was used as an internal standard (-1.318V vs Fc+/Fc). (7) IR (KBr) Y (between 1000 and 1600 cm-I): 1552 (s), 1480 (m), 1466 (m), 1402 (s), 1384 (m), 1353 (m), 1307 (s), 1284 (s), 1212 (m), 1151 (s) cm-I. UV-vis-NIR (toluene): 292 (9200 M-’ cm-I), 475 (2600),513 (2600), 564 (1800),854 (460),975 (390),1304 (480),2340 (5100)nm. (8) (a) Ernst, S.;Hanel, P.; Jordanov, J.; Kaim, W.; Kasack, V.; Roth, E. J. J . Am. Chem. SOC.1989, 111, 1733. (b) Haga, M.;Isobe, K.; Bwne, S. R.; Pierpont, C. G. Inorg. Chem. 1990, 29, 3795. (c) Dei, A,; Gatteschi, D.; Pardi, L.; Russo, U. Inorg. Chem. 1991, 30, 2589. (9) Lever, A. B. P.; Auburn, P. R.; Dodsworth, E. S.;Haga, M.; Liu, W.; Melnik, M.; Nevin, W. A. J . Am. Chem. SOC.1988, 110, 8076. (10) (a) Bhattacharya, S.;Pierpont, C. G. Inorg. Chem. 1992,31, 35. (b) Bhattacharya, S.;Pierpont, C. G. Inorg. Chem. 1991, 30, 2906. (c) Bhattacharya, S.;Pierpont, C. G. Inorg. Chem., submitted for publication.

0 1992 American Chemical Society

J. Am. Chem. SOC.1992, 114, 6583-6585

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Figure 2. Infrared spectrum of Ir(l,5-COD)(3,6-DBCat)2 recorded as a KBr pellet showing the normal ligand vibrational bands at low energy and an electronic transition centered a t 4200 cm-I. Band asymmetry is due to moisture in the KBr; a single symmetrical transition is observed for the complex in solution.

pearing as two quinone ligand-based redox couples that most closely resemble the couples of Fe(bpy)(3,6-DBSQ)(3,6-DBCat).11 Structural features of the molecule, with the anisotropy and absence of ligand proton hyperfine coupling of the EPR spectrum, show that the electronic description is not purely that of the Ir(II1) form,2 however. Interligand charge transfer between catecholate donor and olefm acceptor orbitals exists as a third possibility for the low-energy transition.I2 Two features of the complex may be indirectly related to this assignment. Synergistic interligand s donor-acceptor bonding would remove charge from the catecholate C-0 antibonding orbital. This may contribute to the shorter C-0 length for oxygen atoms bonded trans to Ir-olefin bonds and the relatively long C-C bonds for the coordinated olefin groups. Second, it was of interest to investigate the counterligand dependence of the low-energy transition. Attempts to replace the 1,5-COD ligand with CO, DIPHOS, and 2,2'-bipyridine have all failed.I3 The 1,S-COD ligand is tightly bound to the high oxidation state metal, although the Ir-C lengths to the olefin carbon atoms are not unusually shortI4 and the trans Ir-0 length is identical to the length at the positions cis to the olefin bonds. This is in contradistinction to the catecholate-nitrosyl bonding in Ir(NO)(PPh3)(Br4Cat)where cooperative trans donor-acceptor coordination resulted in shortening of both trans Ir-N and Ir-0 bonds.ls Whether or not it is responsible for the low-energy electronic transition, interligand bonding between the catecholate and olefin ligands of Ir(l,5-COD)(3,6-DBCat)2may be an important ligand stabilization effect. Further studies on coligand bonding effects within the IrL2(Cat)2 series will provide more detailed information on the origin (1 1) Fe(bpy)(3,6-DBSQ)(3,6-DBCat) undergoes oxidation at -0.319 V and reduction at -0.831 V (vs Fc+/Fc). Both are reversible one-electron processes that will be described in a separate publication. (12) Benedix. R.; Hennig, H.; Kunkely, H.; Vogler, A. Chem. Phys. Left. 1991, 175, 483. (13) In typical experiments, Ir( 1,5-COD)(3,6-DBCat), (0.05 g) was refluxed in toluene for the period of 1 day in the presence of an excess of either 2,2'-bipyridine or 1,2-bis(diphenyIphosphino)ethane (DIPHOS) or with CO bubbled through the solution. Electronic spectra obtained on these solutions at the conclusion of the experiment indicated the presence of unreacted Ir(1 ,5-COD)(3,6-DBCat),. (14) See, for examples: (a) Basson, S. S.; Leipoldt, J. G.;Purcell, W.; Schoeman, J. B. Acra Crysrallogr. 1989, C45, 2000. (b) Bright, T. A,; Jones, R. A.; Koschmieder, S. U.; Nunn, C. M. Inorg. Chem. 1988, 27, 3819. (15) Shorthill, W. B.; Buchanan, R. M.; Pierpont, C. G.; Ghedini, M.; Dolcetti, G. Inorg. Chem. 1980, 19, 1803.

of this unusual transition. Acknowledgment. Support for the research carried out at the University of Colorado was provided by the National Science Foundation through Grant C H E 90-23636. We wish to thank Professor G. A. Abakumov for providing the sample of 3,6-ditert-butyl-l,2-benzoquinone used in this investigation. Iridium salts were provided by Johnson-Matthey, Inc., through their Metal Loan Program. Supplementary Material Available: Tables giving crystal data and details of the structure determination, atomic coordinates, anisotropic thermal parameters, hydrogen atom locations, and bond lengths and angles for Ir( 1,5-COD)(3,6-DBCat)2 (9 pages); tables of observed and calculated structure factors ( 6 pages). Ordering information is given on any current masthead page.

A Solid-state 2HNMR Relaxation Study of a 12 Base Pair RNA Duplex Andy C. Wang,' Michael A. Kennedy,tvl Brian R. Reid,'%$ and Gary P. Drobny*sl Department of Biochemistry University of Washington Seattle, Washington 981 95 Department of Chemistry University of Washington Seattle, Washington 981 95 Battelle Pacific Northwest Laboratories Richland. Washington 99352 Received September 9, 1991

In a recent attempt to determine the solution-state structure of a 12 base pair DNA-RNA-DNA chimera ([d(CGCG)r(AAUU)d(CGCG)],), Wang et al.' found that the nonselective IH T Irelaxation times of the RNA were significantly longer than

'

Department of Biochemistry, University of Washington Seattle, WA 98195. *Department of Chemistry, University of Washington Seattle, WA 98195. f Battelle Pacific Northwest Laboratories Richland, WA 99352.

0002-7863/92/1514-6583$03.00/00 1992 American Chemical Societv